Senior C&Q Specialist — Pharma Validation

Veg Group; Juncos (PR); On-site; USD 90,000 - 140,000; Full time

Job summary

Validation & Engineering Group, Inc. is seeking C&Q specialists to support equipment and systems in a biopharmaceutical facility. The specialists will execute field activities, document results, and work with project teams to complete system qualification.

Responsibilities include developing, reviewing, and executing commissioning and qualification protocols, performing field walkdowns, installation verification, and functional testing. Strong GMP knowledge and documentation control are required.

Qualifications

• At least 5 years of C&Q experience in a pharmaceutical or biopharmaceutical facility.
• Experience with FAT, SAT, IQ, OQ, or comparable commissioning and qualification activities.
• Working knowledge of GMP requirements and controlled documentation.
• Strong field execution, technical writing, and teamwork skills.

Responsibilities

• Develop, review, and execute commissioning and qualification protocols.
• Perform field walkdowns, installation verification, and functional testing.
• Review drawings, specifications, and vendor documentation against installed systems.
• Document test results, investigate discrepancies, and support corrective actions.
• Coordinate with Engineering, Operations, and Quality to complete qualification and system turnover.

Skills

C&Q

Field execution

Technical writing

Teamwork

Job description

Validation & Engineering Group, Inc. is seeking C&Q specialists to support equipment and systems in a biopharmaceutical facility. The specialists will execute field activities, document results, and work with project teams to complete system qualification.

Responsibilities include developing, reviewing, and executing commissioning and qualification protocols, performing field walkdowns, installation verification, and functional testing. Strong GMP knowledge and documentation control are required.